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作 者:杨慈清[1,2,3] 李小英[1] 卢习[3] 付苏雷[1] 赵善廷[3] 林俊堂[1,2]
机构地区:[1]新乡医学院生命科学技术学院 [2]河南省医用组织再生重点实验室,新乡453003 [3]西北农林科技大学动物医学院,杨凌712100
出 处:《解剖学杂志》2013年第2期170-172,F0004,共4页Chinese Journal of Anatomy
基 金:国家自然科学基金(31000475);新乡医学院重点研究领域招标课题(ZD201126)
摘 要:目的:建立小鼠子宫内电转基因技术,比较分析转染绿色荧光蛋白(GFP)后对胚胎发育及相关蛋白表达的影响。方法:将怀孕15d的小鼠,水合氯醛麻醉后,取出两侧子宫,用毛细管注射针将2μg/μl的pCAGGS-GFP质粒0.5-1μl准确注射到胎鼠侧脑室,在电压40V、每次脉冲60ms,间隔940ms,电脉冲6次的条件下进行定时定位活体电转基因,电转后24h取材,甲醛固定冷冻冠状切片,DAPI染细胞核观察组织形态结构变化,荧光免疫组织化学检测α-SMA的表达差异。结果:妊娠15d孕鼠转染24h后小鼠成活率80%(8/10),胚胎成活率为54.2%(13/24),存活胚胎GFP阳性表达率为61.5%(8/13),GFP阳性表达胚胎脑组织切片,基因转染区域和正常组织区组织形态结构和α-SMA表达不存在差别。结论:成功建立了小鼠子宫内电转基因的方法。Objective: To construct the method of mouse in utero electroporation, and compare the impact of gene green fluo reseent protein (GFP) on embryonic development and protein expression after transfection. Methods: Pregnancy 15 d mice were selected, and the abdominal cavity was opened after chloral hydrate anesthesia. After 0. 5-1μl plasmid of pCAGGS-GFP was injected into the lateral ventricle of the embryonic brain, 2 uteri were electroporated under the condition of volt 40 V, pulse 60 ms, pause 940 ms for six times. In 24 h after electroporation, mouse embryos were collected and fixed with formalde- hyde, finally cut into frozen coronal slice, DAPI was used to stain nuclei showing morphology changes, and fluorescence im munoassay was carried out with the detection of α-SMA expression differences. Results: 10 mice samples were checked after transfection for 24 h with in utero electroporation, after the mice survival rate was 80% (8/10), embryo survival rate was 54. 2 % (13/24), survival embryonic GFP-positive expression rate was 61.5% (8/13), and the embryonic brains with GFP-positive ex- pression were sliced for further analysis. Compared the GFP positive and normal regions in the brain, the morphology, organization and ccSMA expression did not show changes. Conclusion: The method of the in utero electroporation was constructed successfully.
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